Production Pharmacist (Packaging) JHB

MVG Recruitment; Johannesburg; In loco; ZAR 600.000 - 900.000; Tempo pieno

Descrizione del lavoro

MVG Recruitment is seeking a Production Pharmacist (Packaging) in Midrand, Gauteng. The role provides GMP and regulatory oversight within a pharmaceutical production environment.

The ideal candidate holds a B.Pharm and SAPC registration with 3–5 years of manufacturing experience in solid dosage, liquids, creams or sterile products. You will review batch records, lead deviations and CAPA, and develop GMP documentation.

Competenze

• B.Pharm degree with SAPC registration.
• 3–5 years pharmaceutical manufacturing experience.
• Experience in solid dosage, liquids, creams and/or sterile manufacturing.
• Strong knowledge of GMP and SAHPRA regulations.

Mansioni

• Ensure GMP, quality and regulatory compliance within production and packaging operations.
• Review batch records and production documentation.
• Lead deviation investigations and CAPA implementation.
• Develop and maintain SOPs and GMP documentation.
• Support audits, inspections, validation and continuous improvement initiatives.
• Train and develop production teams on GMP and compliance requirements.

Conoscenze

GMP knowledge

Regulatory oversight

CAPA investigations

Root cause analysis

SOP development

Validation activities

Documentation control

Formazione

B.Pharm degree

Descrizione del lavoro

Production Pharmacist (Packaging)

Midrand, Gauteng | Permanent | Market Related

Ref: MVG/PROD | Closing Date: 27 October 2026

A leading pharmaceutical manufacturer is seeking a Production Pharmacist (Packaging) to provide GMP and regulatory oversight within a pharmaceutical production environment.

Key Requirements:

• B.Pharm degree and SAPC registration
• 3-5 years' pharmaceutical manufacturing experience
• Experience in solid dosage, liquids, creams and/or sterile manufacturing
• Strong knowledge of GMP, SAHPRA regulations, PIC/S and batch documentation
• Experience with SOP development, deviations, CAPA, root cause analysis and validation activities

Key Responsibilities:

• Ensure GMP, quality and regulatory compliance within production and packaging operations
• Review batch records and production documentation
• Lead deviation investigations and CAPA implementation
• Develop and maintain SOPs and GMP documentation
• Support audits, inspections, validation and continuous improvement initiatives
• Train and develop production teams on GMP and compliance requirements

If you are passionate about pharmaceutical quality, compliance and operational excellence, we'd like to hear from you.